Canonical Allele Identifier: CA1385030539

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879044_93879045delinsCT , CM000665.2:g.93879044_93879045delinsCT	GRCh38
NC_000003.11:g.93597888_93597889delinsCT , CM000665.1:g.93597888_93597889delinsCT	GRCh37
NC_000003.10:g.95080578_95080579delinsCT	NCBI36
NG_009813.1:g.100046_100047delinsAG , LRG_572:g.100046_100047delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1644+118_1644+119delinsAG	ENSP00000330021.7:n.1644+118_1644+119delinsAG
ENST00000394236.9:c.1644+118_1644+119delinsAG MANE Select	ENSP00000377783.3:n.1644+118_1644+119delinsAG
ENST00000407433.6:c.1599+118_1599+119delinsAG	ENSP00000385794.2:n.1599+118_1599+119delinsAG
ENST00000647936.1:c.1644+118_1644+119delinsAG	ENSP00000496822.1:n.1644+118_1644+119delinsAG
ENST00000648381.1:n.1812+118_1812+119delinsAG
ENST00000648853.1:c.1602+118_1602+119delinsAG	ENSP00000497262.1:n.1602+118_1602+119delinsAG
ENST00000649103.1:c.1743+118_1743+119delinsAG	ENSP00000497962.1:n.1743+118_1743+119delinsAG
ENST00000649585.1:c.587+118_587+119delinsAG	ENSP00000498163.1:n.587+118_587+119delinsAG
ENST00000650591.1:c.1740+118_1740+119delinsAG	ENSP00000497376.1:n.1740+118_1740+119delinsAG
ENST00000394236.7:c.1644+118_1644+119delinsAG	ENSP00000377783.3:n.1644+118_1644+119delinsAG
ENST00000407433.5:c.1251+118_1251+119delinsAG	ENSP00000385794.1:n.1251+118_1251+119delinsAG
NM_000313.3:c.1644+118_1644+119delinsAG , LRG_572t1:c.1644+118_1644+119delinsAG	NP_000304.2:n.1644+118_1644+119delinsAG
NM_001314077.1:c.1740+118_1740+119delinsAG , LRG_572t2:c.1740+118_1740+119delinsAG	NP_001301006.1:n.1740+118_1740+119delinsAG
NM_000313.4:c.1644+118_1644+119delinsAG MANE Select	NP_000304.2:n.1644+118_1644+119delinsAG
NM_001314077.2:c.1740+118_1740+119delinsAG	NP_001301006.1:n.1740+118_1740+119delinsAG